| Index | PMID | Date | Reference |
|---|---|---|---|
| 1 | 22039503 | 2011 | Zhang, A. M., Bandelt, H. J., Jia, X., Zhang, W., Li, S., Yu, D., Wang, D., Zhuang, X. Y., Zhang, Q., Yao, Y. G. (2011) Is mitochondrial tRNA(phe) variant m.593T>C a synergistically pathogenic mutation in Chinese LHON families with m.11778G>A? PLoS One . 6 (10): e26511 . |
| 2 | 22110754 | 2011 | Zhang, A. M., Jia, X., Bi, R., Salas, A., Li, S., Xiao, X., Wang, P., Guo, X., Kong, Q. P., Zhang, Q., Yao, Y. G. (2011) Mitochondrial DNA haplogroup background affects LHON, but not suspected LHON, in Chinese patients PLoS One . 6 (11): e27750 . |
| 3 | 28579530 | 2017 | Chen, X., Nie, Z., Wang, F., Wang, J., Liu, X. W., Zheng, J., Guo, Y. F., Guan, M. X. (2017) Late onset nonsyndromic hearing loss in a Dongxiang Chinese family is associated with the 593T>C variant in the mitochondrial tRNA(Phe) gene Mitochondrion . 35 (): 111-118 . |
| 4 | 31965079 | 2020 | Wong, L. C., Chen, T., Wang, J., Tang, S., Schmitt, E. S., Landsverk, M., Li, F., Wang, Y., Zhang, S., Zhang, V. W., Craigen, W. J. (2020) Interpretation of mitochondrial tRNA variants Genetics in Medicine 22 (5): 917-926; Suppl Table 1 . |
| 5 | 33552719 | 2021 | Ding, Y., Zhuo, G., Guo, Q., Li, M. (2021) Leber's hereditary optic neuropathy: the roles of mitochondrial transfer RNA variants PeerJ . 9 (): e10651 . |
| 6 | 34053002 | 2022 | Shuai, J., Shi, J., Liang, Y., Ji, F., Gu, L., Yuan, Z. (2022) Mutational analysis of mitochondrial tRNA genes in 138 patients with Leber's hereditary optic neuropathy Irish Journal of Medical Science 191 (2): 865-876 . |
| 7 | 34120304 | 2022 | Finsterer, J. (2022) tRNA variants causing Leber's hereditary optic neuropathy? Irish Journal of Medical Science . 191 (3): 1443-1444 . |